Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/04—Layered products comprising a layer of synthetic resin as impregnant, bonding, or embedding substance
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/38—Layered products comprising a layer of synthetic resin comprising epoxy resins
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
  • C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
  • C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
  • C08G59/4284—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof together with other curing agents
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
  • C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
  • C08G59/62—Alcohols or phenols
  • C08G59/621—Phenols
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
  • C08G59/68—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used
  • C08G59/686—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used containing nitrogen
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
  • C08G59/68—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used
  • C08G59/688—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used containing phosphorus
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
  • C08J5/0405—Reinforcing macromolecular compounds with loose or coherent fibrous material with inorganic fibres
  • C08J5/042—Reinforcing macromolecular compounds with loose or coherent fibrous material with inorganic fibres with carbon fibres
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/24—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
  • C08J5/241—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs using inorganic fibres
  • C08J5/243—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs using inorganic fibres using carbon fibres
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2363/00—Characterised by the use of epoxy resins; Derivatives of epoxy resins

Definitions

• the present invention relates to a two-pack epoxy resin composition used for fiber-reinforced composite materials, a curing agent pack used for this two-pack epoxy resin composition, and a fiber-reinforced composite material produced therefrom.
• Fiber-reinforced composite materials are manufactured by applying the prepreg method, hand lay-up method, filament winding method, pultrusion method, resin transfer molding (RTM) method and other methods.
• the two packs have low and similar viscosity values and exhibit excellent mixability during the mixing work to prepare a resin composition.
• the resin composition exhibits low viscosity during the impregnation of the reinforcing-fiber base and the rise in viscosity can be suppressed throughout this step to ensure excellent impregnability.
• sufficiently fast curing is possible in the low temperature region around 100°C.
• an epoxy resin composition based on a combined use of an acid anhydride and phenol novolac as a curing agent has been disclosed. Since it suppresses the generation of formalin and provides moldings with excellent rigidity, it is preferable as a sheet molding compound for building materials (patent document 1). However this material does not have adequate fast curing performance in the low temperature region.
• an epoxy resin composition based on a combined use of an acid anhydride curing agent and an organic phosphorus compound catalyst has been disclosed as an epoxy resin composition with an excellent balance between the length of the low viscosity period and that of curing time under constant temperature conditions around 100°C (patent document 2).
• this material has a problem in that it is inadequate in fast curing performance and lacks adequate resin rigidity during demolding, sometimes resulting in reduced dimensional accuracy.
• an epoxy resin composition based on the use of a small amount of a carboxylic acid anhydride as an auxiliary catalyst in combination with a phenolic curing agent has been disclosed as an epoxy resin composition for electrical materials that has simultaneously achieved high heat resistance, high toughness and high adherence to copper foils (patent document 3).
• this material also fails to have adequate fast curing performance, while being unsuitable for molding applications due to its need for a solvent.
• the present invention aims to provide a two-pack epoxy resin composition that offers excellent workability during resin preparation, maintains low viscosity during the impregnation of reinforcing fibers, thus exhibiting excellent impregnability, is quickly cured during molding and provides fiber-reinforced composite materials with high dimensional accuracy, a curing agent pack, and a fiber-reinforced composite material produced therefrom by overcoming the shortcomings of prior art.
• the two-pack epoxy resin composition for fiber-reinforced composite materials of the present invention has a specific constitution.
• the two-pack epoxy resin composition for fiber-reinforced composite materials comprises components [A] to [D] as specified below, with component [D] being a liquid at room temperature or a solid having a melting point of 130°C or less.
• component [C] of such a two-pack epoxy resin composition for fiber-reinforced composite materials be a phenol novolac with a softening point of 100°C or less or a cresol novolac with a softening point of 100°C or less.
• component [B] of such a two-pack epoxy resin composition for fiber-reinforced composite materials be an acid anhydride having an alicyclic structure.
• such a two-pack epoxy resin composition for fiber-reinforced composite materials have a specific temperature T at which 0.5 ⁇ t10 ⁇ 4, 0.5 ⁇ t90 ⁇ 9 and 1 ⁇ t90/t10 ⁇ 2.5 hold, where t10 and t90 are lengths of time (in minutes) that the cure index, as obtained in a dielectric measurement performed while maintaining a constant temperature, takes to reach 10% and 90%, respectively.
• such a two-pack epoxy resin composition for fiber-reinforced composite materials be obtained by mixing a base resin pack comprising component [A] and a curing agent pack comprising components [B], [C] and [D].
• the curing agent pack of such a two-pack epoxy resin composition for fiber-reinforced composite materials have a viscosity at 25°C of 0.05 to 1.8 Pa ⁇ s.
• a fiber-reinforced composite material of the present invention has a specific configuration. Namely, the fiber-reinforced composite material is produced by combining the above two-pack epoxy resin composition for fiber-reinforced composite materials with reinforcing fibers and curing it.
• the present invention makes it possible to provide fiber composite materials having high dimensional accuracy with high productivity, thanks to excellent workability during resin preparation, excellent resin impregnability based on the retention of low viscosity during the impregnation of reinforcing fibers and fast curing during the molding step.
• component [A] under the present invention include an aromatic glycidyl ether obtained from a phenol having two or more hydroxyl groups, an aliphatic glycidyl ether obtained from an alcohol having two or more hydroxyl groups, a glycidyl amine obtained from an amine, an epoxy resin having an oxirane ring, and a glycidyl ester obtained from a carboxylic acid having two or more carboxyl groups.
• Examples of a glycidyl amine available for use as component [A] under the present invention include diglycidyl aniline, diglycidyl toluidine, triglycidyl aminophenol, tetraglycidyl diaminodiphenyl methane, tetraglycidyl xylylene diamine, and a halogen or alkylic substitution product or hydrogenated product thereof.
• Examples of an epoxy resin having an oxirane ring available for use as component [A] under the present invention include vinyl cyclohexene dioxide, dipentene dioxide, 3,4-epoxycyclohexane carboxylic acid 3,4-epoxycyclohexylmethyl, adipic acid bis(3,4-epoxycyclohexylmethyl), dicyclopentadiene dioxide, bis(2,3-epoxycyclopentyl) ether, and an oligomer of 4-vinyl cyclohexene dioxide.
• a diglycidyl ether of a bisphenol compound namely a bisphenol-type epoxy resin, especially a bisphenol A-type epoxy resin
• component [A] is particularly advantageously used as component [A] under the present invention as it excels in terms of the balance between the viscosity of the resin composition and the mechanical and physical properties of the cured resin product obtained, such as heat resistance and elastic modulus. It is preferable that such component [A] account for 60 to 100, more preferably 80 to 100, mass% of the total epoxy resin.
• component [B] is an acid anhydride, specifically a carboxylic acid anhydride and more specifically a compound that has one or more carboxylic acid anhydride groups capable of reacting with epoxy groups in an epoxy resin in a single molecule and acts as a curing agent for an epoxy resin.
• Component [B] under the present invention may be an acid anhydride that, like a phthalic anhydride, has an aromatic ring but does not have an alicyclic structure or an acid anhydride that, like a succinic anhydride, has neither an aromatic ring nor an alicyclic structure.
• an acid anhydride having an alicyclic structure with one having a cycloalkane or cycloalkene ring preferred.
• Such an acid anhydride having an alicyclic structure include a hexahydro phthalic anhydride, methyl hexahydro phthalic anhydride, methyldihydro nadic anhydride, 1,2,4,5-cyclopentane tetracarboxylic dianhydride, 1,2,3,6-tetrahydrophthalic anhydride, methyl-1,2,3,6-tetrahydrophthalic anhydride, nadic anhydride, methyl nadic anhydride, bicyclo[2,2,2]octo-7-ene-2,3,5,6-tetracarboxylic dianhydride, and 4-(2,5-dioxotetrahydrofuran-3-yl)-3-methyl-1,2,5,6-tetrahydrophthalic anhydride.
• hexahydro phthalic anhydride, tetrahydrophthalic anhydride, nadic anhydride and a selected alkyl substitution product thereof are particularly advantageously used as component [B] under the present invention, as they excel in terms of the balance between the viscosity of the resin composition, on the one hand, and the heat resistance and the elastic modulus and other mechanical and physical properties of the cured resin product, on the other.
• the epoxy resin composition of the present invention may contain acid anhydrides without an alicyclic structure.
• component [C] is a compound that has an average of 2.5 or more hydroxyphenyl structures in each molecule. More specifically, it is a compound whose chemical structure has an average of 2.5 or more structures containing phenol as illustrated in chemical formula 2 in each molecule, and acts as a curing agent for an epoxy resin.
• the average number of such hydroxyphenyl structures is on a weight equivalent basis.
• a typical method for phenol novolac and other compounds having a distribution in the number of repeating units for instance, uses a molecular weight distribution chart obtained from gel permeation chromatography (GPC) and calculates the ratio between peak areas, each corresponding to the number of repeating units.
• GPC gel permeation chromatography
• phenol resins such as a phenol novolac resin, phenol aralkyl resin, biphenyl novolac-type phenol resin, cresol novolac resin, naphthol novolac resin, tris-(hydroxyphenyl) methane, tetrakis (hydroxyphenyl) ethane, a terpene backbone-containing phenol compound and dicyclopentadiene backbone-containing phenol resin, are advantageously used.
• phenol novolac, cresol novolac and the like are preferable from the viewpoint of ease of handling and mechanical and physical properties of cured products, with phenol novolac having a softening point of 100°C or less or cresol novolac having a softening point of 100°C or less particularly preferred.
• component [C] in combination with component [B] makes it possible to shorten the time taken to complete curing, while keeping the low viscosity period long, as required of a resin composition for RTM.
• component [B] is functioning as not only a curing agent but also a catalyst for component [C].
• the mixing of the two beforehand tends to make it easier to mix them with component [A] by moderately increasing the viscosity of the curing agent pack.
• an organic phosphorus compound under the present invention examples include tributyl phosphine (liquid at room temperature), trioctyl phosphine (liquid at room temperature), tricyclohexyl phosphine (melting point 82°C), triphenyl phosphine (melting point 80°C), tribenzyl phosphine (melting point 99°C), tri-o-tolyl phosphine (melting point 124°C), tri-m-tolyl phosphine (melting point 98°C), diphenyl cyclohexyl phosphine (melting point 60°C), and 1,3-bis(diphenyl phosphino)propane (melting point 64°C).
• the epoxy resin composition of the present invention have a viscosity at 25°C of 0.1 to 2.5 Pa ⁇ s, more preferably 0.1 to 2.0 Pa ⁇ s. Setting the viscosity at 25°C to 2.5 Pa ⁇ s or less makes it possible to lower the viscosity at the molding temperature and shorten the time required to impregnate the reinforcing-fiber base, thus eliminating the cause for impregnation failure.
• viscosity is determined by measuring the viscosity of the epoxy resin composition immediately after preparation via, for instance, the measuring method that uses a cone-and-plate rotational viscometeras specified in ISO 2884-1 (1999).
• Examples of actual measuring equipment include the model TVE-30H, manufactured by Toki Sangyo Co., Ltd.
• Dielectric measurement is beneficial in obtaining the curing profile of a thermosetting resin as it transforms from a low-viscosity liquid to an amorphous solid with a high elastic modulus, though it is unable to directly measure viscosity or elastic modulus.
• the curing profile of a thermosetting resin is obtained from the change in ion viscosity (equivalent resistivity) with time as calculated from the complex dielectric constant measured by applying a high-frequency electric field.
• the curing monitor model MDE-10 manufactured by Holometrix-Micromet, for instance, is available.
• the procedure begins with the installation of a Viton O-ring with an inside diameter of 32 mm and a thickness of 3 mm on the underside of an MP2000 programmable mini press featuring an embedded-into-the-bottomTMS-1 inch-type sensor and the setting of the temperature of the press to a predetermined value, T.
• An epoxy resin composition is then poured into the hollow inside the O-ring.
• the press is closed, the change in the ion viscosity of the resin composition with time is tracked.
• a dielectric measurement is performed at frequencies of 1, 10, 100, 1000 and 10000Hz, and the frequency-independent logarithm Log( ⁇ ) of ion viscosity is obtained using the software bundled with the equipment (Yu metric).
• the cure index at the required curing time, t is obtained using expression 4, with the times at which the cure index reaches 10% and 90% denoted as t10 and t90, respectively.
• Cure index log ⁇ t - log ⁇ min / log ⁇ max - log ⁇ min ⁇ 100
• t10 which is proportional to the time required for an epoxy resin composition to become fluid at the specific temperature T (fluidizability time) is 0.5 to 4 minutes (expression 1).
• t90 which is proportional to the time required for the curing of an epoxy resin composition to complete to allow demolding (demoldability time), is 0.5 to 9 minutes (expression 2).
• the ratio between the fluidizability time and demoldability time of an epoxy resin composition is more than 1 and 2.5 or less (expression 3).
• t90/t10 be as small as possible within the range of 1 (exclusive) to 2.5 (inclusive).
• the molding temperature (thermal curing temperature) of an epoxy resin composition namely the specific temperature T
• the specific temperature T be within the90 to 130°C range. Setting the specific temperature T within the90 to 130°C range makes it possible to obtain a fiber-reinforced composite material with good surface quality by simultaneously shortening the time required for curing and alleviating the post-demolding heat shrinkage.
• the two-pack epoxy resin composition of the present invention is obtained by first preparing a base resin pack containing an epoxy resin, labeled component [A], as the primary component and a curing agent pack containing curing agents, labeled components [B] and [C], as the secondary components at the blending quantities specified above and, immediately before use, mixing them while adhering to the specified blending quantities.
• component [D] may be blended into either the base resin pack or curing agent pack, it is more preferable that it be included in the curing agent pack.
• Other blending components may be blended into whichever pack, so that they may, in advance, be blended into either the base resin pack or curing agent pack, or even both.
• the curing agent pack for fiber-reinforced composite materials of the present invention comprise component [B], [C] and [D]. It is preferable that the viscosity at 25°C of such a curing agent pack for fiber-reinforced composite materials be 0.05 to 1.8 Pa ⁇ s, more preferably 0.05 to 0.7 Pa•s. This is because setting the viscosity of the curing agent pack to 1.8 Pa ⁇ s s or less makes it possible to shorten the reinforcing fiber impregnation time and eliminate the cause of impregnation failure by making the viscosity of the resin composition at the molding temperature low.
• the viscosity of the curing agent pack makes it possible to avoid pitting, attributable to the trapping of air during the impregnation of the reinforcing-fiber base, and prevent the generation of unimpregnated regions, attributable to uneven impregnation, by keeping the viscosity at the molding temperature sufficiently high. It is advisable that the base resin pack and curing agent pack be separately heated before mixing and it is also preferable that they be mixed to obtain an epoxy resin composition immediately before use, e.g. injection into a mold, using a mixer from the viewpoint of the handleable period of the resin.
• the procedure to produce a fiber-reinforced composite material of the present invention is described.
• the epoxy resin composition of the present invention is obtained in the manner described above. It is preferable that a fiber-reinforced composite material of the present invention be produced by preheating the epoxy resin composition, injecting it into a mold that has been preheated to the specific temperature T and holding a reinforcing-fiber base to impregnate the fibers, and curing the resin inside the mold.
• the temperature at which to heat the epoxy resin composition to be determined from the relationship between the initial viscosity of the epoxy resin composition and the rise in viscosity, be 40 to 70°C, more preferably 50 to 60°C, from the viewpoint of the impregnability of the reinforcing-fiber base.
• the injection pressure of the epoxy resin composition is usually 0.1 to 1.0 MPa.
• VaRTM vacuum-assisted resin transfer molding
• the injection pressure be 0.1 to 0.6 MPa from the viewpoint of injection time and economic efficiency of equipment. It is also preferable that, even in the case of using compression injection, the mold be vacuum-aspirated before the injection of the resin composition to suppress the generation of voids.
• fiber-reinforced composite material of the present invention glass fiber, aramid fiber, carbon fiber, boron fiber and the like are advantageously used as reinforcing fibers.
• carbon fiber is particularly advantageous for the reason that it makes it possible to obtain fiber-reinforced composite materials that excel in strength, elastic modulus and other mechanical and physical properties, despite being lightweight.
• Reinforcing fibers may be either short fibers or continuous fibers or even a combination of both. To obtain a fiber-reinforced composite material with a high Vf, continuous fibers are preferable.
• reinforcing fibers are sometimes used in strand form, but reinforcing-fiber bases made of reinforcing fibers worked into a mat, woven fabric, knit fabric, braid, unidirectional sheet or a similar form are advantageously used.
• woven fabrics are particularly advantageous as they are suited to producing high-Vf fiber-reinforced composite materials and are excellent in handleability.
• the ratio of the net reinforcing fiber volume of a woven fabric to its apparent volume is defined as the fiber packing ratio of a woven fabric.
• the fiber packing ratio of a woven fabric is obtained from the weight per unit surface area of the woven fabric W (unit: g/m 2 ), thickness t (unit: mm) and density of the reinforcing fiber pf(unit: g/cm 3 ) based on the expression W/(1000t ⁇ pf).
• the surface-area weight density (weight per unit surface area) and thickness of the woven fabric are obtained in accordance with JIS R 7602(1995).
• the fiber packing ratio of a woven fabric be within the 0.10 to 0.85, preferably 0.40 to 0.85 and more preferably 0.50 to 0.85, range.
• volume fraction of fiber Vf be in the 40 to 85%, preferably 45 to 85%, range.
• the volume fraction of fiber Vf of a fiber-reinforced composite material as specified here is a value defined and measured as shown below in accordance with ASTM D3171(1999) and applies to the post-impregnation and post-curing state.
• the volume fraction of fiber Vf of a fiber-reinforced composite material can be obtained from thickness h using the expression below.
• Vf % Af ⁇ N / ⁇ f ⁇ h / 10
• Af Weight of fiber base per unit area (g/m 2 )
• N Number of laminated fiber bases
• ⁇ f Density of reinforcing fiber (g/cm 3 )
• h Thickness of fiber-reinforced composite material (test piece) (mm).
• the volume fraction of fiber of a fiber-reinforced composite material is measured using any of the combustion method, nitric acid decomposition method and sulfuric acid decomposition method as specified in JIS K 7075 (1991). In such cases, the value of the density of the reinforcing fiber used should be one measured in accordance with JIS R 7603 (1999).
• One of the preferable forms of a fiber-reinforced composite material of the present invention is a veneer.
• Other preferable forms include a sandwich structure, in which veneer-like fiber-reinforced composite materials are placed against a core material on two opposing sides, and a hollow structure, in which veneer-like structures are joined in a closed chain to leave a hollow inside, and a canagings structure, in which a veneer-like fiber-reinforced composite material is placed against a core material on one side.
• Examples of a core material in a sandwich structure or cana regards structure include an aluminum or aramid honeycomb core, a polyurethane, polystyrene, polyamide, polyimide, polyvinyl chloride, phenol resin, acrylic resin, epoxy resin or other formed plastic core, or a balsa or other wooden core.
• a formed plastic core is particularly advantageously used as a core material for the reason that it makes it possible to obtain a lightweight fiber-reinforced composite material.
• epoxy resin composition of the present invention is described in further detail below using examples.
• Various base resin packs were obtained by mixing epoxy resins at compounding ratios specified in Tables 1 and 2.
• Various curing agent packs were obtained by mixing an acid anhydride, a compound that has an average of 2.5 or more hydroxyphenyl structures in each molecule and a curing accelerator at compounding ratios specified in Tables 1 and 2.
• each epoxy resin composition was measured using a measuring method based on a cone-and-plate rotational viscometer in accordance with ISO 2884-1 (1999).
• the actual equipment chosen was a TVE-30H from Toki Sangyo Co., Ltd. with a 1°34' ⁇ R24 rotor.
• the sample quantity was 1 cm 3 .
• a dielectric measurement was conducted.
• an MDE-10curing monitor from Holometrix-Micromet was chosen. The procedure began with the installation of a Viton O-ring with an inside diameter of 32 mm and a thickness of 3 mm on the underside of an MP2000 programmable mini press featuring an embedded-into-the-bottom TMS-1 inch-type sensor and the setting of the temperature of the press to 100°C.
• An epoxy resin composition was then poured into the hollow inside the O-ring. After the press was closed, the change in the ion viscosity of the resin composition with time was tracked.
• a dielectric measurement was performed at frequencies of 1, 10, 100, 1000 and 10000Hz, and the frequency-independent logarithm Log( ⁇ ) of ion viscosity was obtained using the software bundled with the equipment.
• a 2 mm-thick copper spacer produced by making a hole in the middle of a 50 mm-square specimen was installed on the underside of the press equipment, and the press temperature was set to 110°C. An epoxy resin composition was then poured through the hole of the spacer, and the press was closed. Twenty minutes later, the press was opened, and a cured resin plate was obtained.
• a test piece 12.7mm wide and 40mm long was cut out of the cured resin plate, and a torsional DMA measurement was conducted using a rheometer (ARES manufactured by TA Instruments). As a measurement condition, the heating speed was set to 5°C/min. The temperature at which the storage modulus curve obtained in the measurement had an inflection point G' was denoted as Tg.
• the void content of a molding is a quantity measured by observing a smoothly polished cross section of the molding using an incident-light microscope and calculating the proportion of the combined area accounted for by voids.
• An epoxy resin composition was prepared and then subjected to a viscosity measurement and dielectric measurement as described above.
• a cured resin plate and fiber-reinforced composite material were prepared in the manner described above using the prepared epoxy resin composition.
• epoxy resin compositions that fall outside the range set by the present invention do not have satisfactory characteristics.
• the cured resin product has a low Tg compared to the working examples and is inferior in terms of the demoldability of the fiber-reinforced composite material.
• the viscosity of the curing agent pack is high, resulting in inferior resin mixability, while viscosity stays high even after the mixing of the base resin pack and curing agent pack, resulting in inferior reinforcing fiber impregnability.

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• Chemical & Material Sciences (AREA)
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• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Manufacturing & Machinery (AREA)
• Inorganic Chemistry (AREA)
• Reinforced Plastic Materials (AREA)
• Epoxy Resins (AREA)

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• 2012
  • 2012-10-23 KR KR1020147002999A patent/KR20140097103A/ko not_active Application Discontinuation
  • 2012-10-23 CN CN201280053108.6A patent/CN103917574B/zh not_active Expired - Fee Related
  • 2012-10-23 EP EP12846109.2A patent/EP2774939A4/fr not_active Withdrawn
  • 2012-10-23 JP JP2012555232A patent/JP6007794B2/ja not_active Expired - Fee Related
  • 2012-10-23 US US14/352,342 patent/US9328237B2/en not_active Expired - Fee Related
  • 2012-10-23 WO PCT/JP2012/077299 patent/WO2013065516A1/fr active Application Filing

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